A Phase II Trial of PLX3397 in the Treatment of KIT Mutated Advanced Acral and Mucosal Melanoma
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 7
- 试验地点
- 8
- 主要终点
- Efficacy of PLX3397
研究概览
简要总结
KIT (receptor tyrosine kinase) mutations occur in 15% of acral and mucosal melanomas. PIANO is a single arm, phase II, open-label, multicentre study to evaluate the efficacy and safety (plus molecular basis of such effects) of the KIT inhibitor PLX3397 (developed by Plexxikon) in advanced KIT mutated acral and mucosal melanoma.
In this trial a total of 24 patients (9 in the first stage and 15 in the second stage) will receive treatment over a 24 month recruitment period.
Following consent and successful screening, patients will receive PLX3397 capsules 1000mg/day as monotherapy, and will remain on therapy as long as they are deriving clinical benefit. Patients will be seen every 4 weeks during treatment to monitor response and toxicity. Routine blood tests will be carried out at all visits and pharmacokinetics/pharmacodynamics sampling (1 x 8 milliliter(ml) whole blood sample) will be done pre-dose on Day 1 and Day 15, frozen and stored locally and sent to Plexxikon's vendor for central analysis at the end of the study. Imaging will be carried out every 12 weeks to monitor response. The first 9 patients will also receive two [18F]-fluorodeoxyglucose (FDG) PET scans (baseline and at Day 15).
From specific named participating sites, 12 patients will provide additional (optional) consent to take part in translational research. 5 of these patients will have a fresh tumour biopsy taken at baseline, at day 15 and upon disease progression. The same 5 patients plus an additional 7 patients (to give a total of 12 patients) will also donate blood samples at baseline, 2 weeks, 12 weeks and on disease progression for the evaluation of circulating tumour cells and circulating free tumour DNA.
All patients will be followed up every 6 months until death or for 12 months after the last patient has discontinued study treatment.
详细描述
The PIANO trial is an open-label, single-arm, multicentre phase II trial of PLX3397 in advanced acral and mucosal melanoma. All eligible patients will receive PLX3397 1000mg/day as monotherapy and will remain on treatment as long as they are deriving benefit (at the treating Investigator's discretion).
The primary objective of this study is to assess the efficacy of PLX3397 by review of the number of patients who are progression-free at 6 months. Additional objectives include assessing the safety of PLX3397, overall survival and (for a sub-set of patients) biomarker research.
A maximum of 24 eligible patients may be treated in this study. In order to recruit 24 patients, it is expected that a total of approximately 240 patients will need to be consented and screened for the KIT mutation, as only KIT mutant patients are eligible (and this is estimated to be 10-15% of this patient population). An interim analysis by the Independent Data Monitoring Committee will be done after 9 patients have been recruited and if less than 2 out of the 9 patients have demonstrated progression free survival at 6 months the trial will be terminated.
As only KIT mutant patients are eligible for inclusion, the very first step following consent is for patients' KIT mutation status to be tested. Only patients who have KIT mutations are eligible. Wherever possible, archival tissue samples taken at the time of diagnosis will be requested but if a suitable sample is not available or if following testing no result is obtained an additional fresh tumour sample would be collected via a biopsy. The tissue sample will be sent to specialist laboratories for KIT testing and the results of this test take 1-2 weeks. If the patient is found to have a KIT mutation which is not associated with PLX3397 resistance, they will return to clinic to complete the following study parameters and investigations upto 4 weeks prior to the start of treatment except those examinations which are marked with an (*) ;
- Demographic details
- Medical and surgical history including discussions of current medications
- Tumour evaluation according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria v1.1 using CT or MRI scans of the thorax, abdomen and pelvis within 28 days of scheduled start of treatment
- Vital signs and standard physical examination (to include blood pressure, pulse, temperature, height and weight)*
- Eastern Cooperative Oncology Group (ECOG) performance status*
- Laboratory investigations: full blood count, biochemistry (Urea & Electrolytes, creatinine, calcium, albumin, liver function tests, lactate dehydrogenase (LDH), glucose, phosphate) and clotting screen*
- Women of childbearing potential will have a urine or serum pregnancy test( within 72 hours of study entry)
- Electrocardiograph (ECG)*
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with KIT mutated histologically proven advanced mucosal or acral melanoma in which the mutation is not known to be associated with PLX3397 resistance
- •Unresectable locally advanced or metastatic disease
- •The presence of one or more clinically or radiologically measurable lesions at least 10mm in size
- •ECOG performance status 0, 1 or 2
- •Life expectancy greater than 12 weeks
- •Age 18 or greater
- •Women must be postmenopausal (no menstrual period for a minimum of 1 year) or have a negative serum pregnancy test on entry in the study (even if surgically sterilised). Men and women of childbearing potential must use adequate birth control measures for the duration of the study and should continue such precautions for 3 months after receiving the last dose of study treatment
- •At least 28 days since major surgery and 7 days since skin/tumour biopsy
- •Serum alanine transaminase (ALT) ≤2.5 x upper limit of normal (ULN) or serum aspartate aminotransferase≤2.5 x ULN
- •Total serum bilirubin ≤1.5 x ULN
- •Serum creatinine ≤1.5 x ULN
- •Haemoglobin ≥90 g/L, absolute neutrophil count ≥1.5 x 109/L, platelets ≥100 x 109/L
- •Prothrombin time (PT) ≤1.5 x ULN
- •The ability to swallow and retain oral medication
- •The capacity to understand the patient information sheet and the ability to provide written informed consent
- •Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures
排除标准
- •Intracranial disease, unless there has been radiological evidence of stable intracranial disease > 6 months. In the case of a solitary brain metastasis, evidence of a disease-free interval of at least 3 months post surgery. All patients previously treated for brain metastases must be stable off corticosteroid therapy for at least 28 days
- •Women who are pregnant, nursing, or planning pregnancy within 6 months after the last treatment
- •Men who plan to father a child within 3 months of the last treatment
- •Use of any investigational drug within 30 days prior to screening
- •Significant cardiac disease including patients who have or who are at significant risk of developing prolongation of corrected QT interval (QTc)
- •Severe and/or uncontrolled medical disease
- •Known chronic liver disease
- •Known HIV infection
- •Previous radiotherapy to 25% or more of the bone marrow and/or radiation therapy in the 4 weeks prior to study entry
- •Prior exposure to a KIT inhibitor
- •Patients with KIT mutations that are known to be associated with PLX3397 resistance
- •Use of Chinese or herbal medication
- •Any malabsorption syndrome (i.e. partial gastrectomy, small bowel resection, crohn's disease or ulcerative colitis)
研究组 & 干预措施
PLX3397
Patients will be given PLX3397 1000mg/day as monotherapy. Patients will remain on treatment as long as they are deriving benefit. This is a single cohort study and so there is no comparator arm - all patients receive the same treatment.
干预措施: PLX3397 (Drug)
结局指标
主要结局
Efficacy of PLX3397
时间窗: 6 months
The primary objective of this study is to evaluate the efficacy of PLX3397 in KIT mutated advanced mucosal and acral melanoma as measured by the proportion of study participants tumour progression free at 6 months.
次要结局
- Overall Survival(Participants are followed up for upto an average of 5 years or until the last patient dies, whichever comes first.)
- Safety of PLX3397(minimum of 12 month following stoppage of treatment and for minimum of 5 years for patients remaining on treatment)
- Mechanism of response and resistance to PLX3397(For 12 weeks or until the patient stops treatment)
- Response rate(12 weeks)